Mentions
Extended reach
Total likes
Video views
AI synopsis
Several discussions highlight the innovative nature of the publication, emphasizing the 'fabulous collaboration' and 'efficient entry to new chemical space,' which showcase excitement about advancements in synthetic chemistry. The tone is enthusiastic and technical, illustrating a recognition of the potential to open new pathways in molecular design, though the overall focus remains on methodological breakthroughs rather than immediate societal impact.
Most discussions strongly support the significance of the new synthetic strategy, with phrases like 'fabulous collaboration,' 'efficient entry,' and 'unprecedented structures' indicating enthusiasm and approval.
Posts demonstrate high curiosity and excitement about the chemical process, shown through mentions of 'fabulous collaboration,' 'new chemical space,' and 'unprecedented structures,' which reflect eagerness to understand the novel methodology.
The discussions show deep analysis, with references to specific technical aspects such as 'Nickel/Photoredox Dual Catalysis' and 'three-component transformation,' indicating thoughtful engagement.
While the perceptions are highly positive, some posts hint at the potential for broader applications, but the emphasis remains on the novelty and efficiency rather than immediate real-world impact, suggesting a slightly moderate perceived impact.
Fabulous collaboration with AbbVie leads to an efficient entry to new chemical space in the [1.1.1]bicyclopentane domain. Photoredox/Ni dual catalysis in a three-component transformation provides unprecedented structures. See in @J_A_C_S ASAPs! https://t.co/fcZySVZTn7
Dicarbofunctionalization of Propellane: Ni/Photoredox Dual Catalysis: 1-Step Multicomponent Synthesis of BCP-Aryl Derivatives @molandergroup @PennChemistry @Penn @TotalSyntheses #Dicarbofunctionalization #Propellane #Nickel #Photoredox #Catalysis https://t.co/7GCBWa4Iau
Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives. @J_A_C_S @isciverse #Chemistry #scicomm #news #Technology #Trending #research #science https://t.co/uGslheCSpn https://t.co/6piQ1cq6Tm
JACS online: #Dicarbofunctionalization of [1.1.1]#Propellane Enabled by #Nickel/#Photoredox Dual #Catalysis: One-Step Multicomponent Strategy for the #Synthesis of BCP-Aryl Derivatives @J_A_C_S @molandergroup @PennChemistry @Penn @TotalSyntheses https://t.co/hVDlzvAMTz
Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives https://t.co/gy8yn5pBZS
Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives https://t.co/aKm9sSUX5F
In this video, I discuss five important papers in organic synthesis that were published in June 2022. The trifluoromethyl group is highlighted for its impact on small-molecule drugs, showcasing a new method for…
LHC back in action. The video discusses recent updates on the Large Hadron Collider's return to operation and explores advancements in photoredox catalysis, highlighting key research findings. Please like, comment, and…
https://t.co/60wMptRXlc
[JACS] [ASAP] Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives https://t.co/9Y8DcnpfA8
RT @chem_flow: Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy…
RT @InnovationChem: JACS online: #Dicarbofunctionalization of [1.1.1]#Propellane Enabled by #Nickel/#Photoredox Dual #Catalysis: One-Step…
RT @chem_flow: Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy…
Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives https://t.co/aKm9sSUX5F
RT @InnovationChem: JACS online: #Dicarbofunctionalization of [1.1.1]#Propellane Enabled by #Nickel/#Photoredox Dual #Catalysis: One-Step…
JACS online: #Dicarbofunctionalization of [1.1.1]#Propellane Enabled by #Nickel/#Photoredox Dual #Catalysis: One-Step Multicomponent Strategy for the #Synthesis of BCP-Aryl Derivatives @J_A_C_S @molandergroup @PennChemistry @Penn @TotalSyntheses https://t.co/hVDlzvAMTz
RT @J_A_C_S: Dicarbofunctionalization of Propellane: Ni/Photoredox Dual Catalysis: 1-Step Multicomponent Synthesis of BCP-Aryl Derivatives…
Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives https://t.co/VeTmR4NVP0 #nor論文 いつも同じこと言ってるけど反応のパターンの増え方すごいな
RT @chem_flow: Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy…
Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives https://t.co/aKm9sSUX5F
RT @J_A_C_S: Dicarbofunctionalization of Propellane: Ni/Photoredox Dual Catalysis: 1-Step Multicomponent Synthesis of BCP-Aryl Derivatives…
RT @J_A_C_S: Dicarbofunctionalization of Propellane: Ni/Photoredox Dual Catalysis: 1-Step Multicomponent Synthesis of BCP-Aryl Derivatives…
Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives https://t.co/2OqFagmgDY
RT @J_A_C_S: Dicarbofunctionalization of Propellane: Ni/Photoredox Dual Catalysis: 1-Step Multicomponent Synthesis of BCP-Aryl Derivatives…
RT @molandergroup: Fabulous collaboration with AbbVie leads to an efficient entry to new chemical space in the [1.1.1]bicyclopentane domain…
Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives. @J_A_C_S @isciverse #Chemistry #scicomm #news #Technology #Trending #research #science https://t.co/uGslheCSpn https://t.co/6piQ1cq6Tm
Dicarbofunctionalization of Propellane: Ni/Photoredox Dual Catalysis: 1-Step Multicomponent Synthesis of BCP-Aryl Derivatives @molandergroup @PennChemistry @Penn @TotalSyntheses #Dicarbofunctionalization #Propellane #Nickel #Photoredox #Catalysis https://t.co/7GCBWa4Iau
RT @molandergroup: Fabulous collaboration with AbbVie leads to an efficient entry to new chemical space in the [1.1.1]bicyclopentane domain…
RT @molandergroup: Fabulous collaboration with AbbVie leads to an efficient entry to new chemical space in the [1.1.1]bicyclopentane domain…
RT @molandergroup: Fabulous collaboration with AbbVie leads to an efficient entry to new chemical space in the [1.1.1]bicyclopentane domain…
RT @molandergroup: Fabulous collaboration with AbbVie leads to an efficient entry to new chemical space in the [1.1.1]bicyclopentane domain…
RT @molandergroup: Fabulous collaboration with AbbVie leads to an efficient entry to new chemical space in the [1.1.1]bicyclopentane domain…
RT @molandergroup: Fabulous collaboration with AbbVie leads to an efficient entry to new chemical space in the [1.1.1]bicyclopentane domain…
RT @molandergroup: Fabulous collaboration with AbbVie leads to an efficient entry to new chemical space in the [1.1.1]bicyclopentane domain…
Dicarbofunctionalization of [1.1.1]Propellane Enabled by Nickel/Photoredox Dual Catalysis: One-Step Multicomponent Strategy for the Synthesis of BCP-Aryl Derivatives https://t.co/gy8yn5pBZS
RT @molandergroup: Fabulous collaboration with AbbVie leads to an efficient entry to new chemical space in the [1.1.1]bicyclopentane domain…
Fabulous collaboration with AbbVie leads to an efficient entry to new chemical space in the [1.1.1]bicyclopentane domain. Photoredox/Ni dual catalysis in a three-component transformation provides unprecedented structures. See in @J_A_C_S ASAPs! https://t.co/fcZySVZTn7